Placebo-controlled RCT: After out-of-hospital cardiac arrest, nelonemdaz does not reduce serum neuron-specific enolase levels at 48 to 52 hours.
Chun BJ, Yeom SR, Chung SP, et al. Nelonemdaz Treatment for Patients With Out-of-Hospital Cardiac Arrest: A Randomized Clinical Trial. Crit Care Med. 2025 Jan 16. doi: 10.1097/CCM.0000000000006579.

OBJECTIVES: Nelonemdaz is a N-methyl d-aspartate receptor subtype 2B-selective N-methyl-D-aspartate receptor antagonist and a potent free-radical scavenger that might ameliorate hypoxic-ischemic brain injury after out-of-hospital cardiac arrest (OHCA). We investigated the efficacy of nelonemdaz for patients with OHCA.

DESIGN: A double-blind, placebo-controlled, randomized, multicenter phase II trial.

SETTING: This trial enrolled 105 patients at five sites in South Korea between November 18, 2018, and February 23, 2023.

PARTICIPANTS: OHCA patients undergoing targeted temperature management.

INTERVENTIONS: Patients were randomly assigned to high-dose (5250 mg), low-dose (3250 mg), and placebo groups at a 1:1:1 ratio.

MEASUREMENTS AND MAIN RESULTS: Patients with a median age of 61 years (82% male) were assigned to the high-dose (n = 37), low-dose (n = 35), and placebo (n = 33) groups. The primary outcome, the serum level of neuron-specific enolase (NSE) at 48-52 hours, was evaluated in 93 patients. There was no difference in serum NSE between high-dose (median and interquartile range; 23.7, 15.0-69.9) and placebo (17.5, 13.6-113.0) groups, or between low-dose (26.6, 16.2-83.4) and placebo groups (all p > 0.05). Brain MRI fractional anisotropy was significantly higher in the high-dose group compared with the placebo group (0.465, 0.449-0.485 vs. 0.441, 0.431-0.464; p = 0.028), but not between low-dose (0.462, 0.439-0.480) and placebo groups (p > 0.05). At day 90, the common odds ratio (95% CI) indicating a numerically favorable shift in the modified Rankin Scale was 1.25 (0.48-3.24) and 1.22 (0.47-3.20) in the high-dose and low-dose groups, respectively, compared with placebo group (all p > 0.05). No serious adverse events were reported.

CONCLUSIONS: Nelonemdaz treatment of patients after OHCA did not reduce serum NSE levels compared with controls. Patients treated with high-dose nelonemdaz showed higher brain MRI fractional anisotropy suggesting less cerebral white matter damage.

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Comments from MORE raters

Hospital Doctor/Hospitalists

As an ER physician, I encounter quite a few patients presenting after OHCA. The research on any substance that can reduce oxidative stress and increase survival of neurons is extremely important. I wish the research would also look into effects of nelonemdaz on cardiac muscle.

Internal Medicine

It's exciting to see new medications aimed at reducing neurologic complications of cardiac arrest, but they did not meet the primary outcome and only showed a trend toward clinical improvement. The positive finding for better ADC damage volume is a surrogate outcome. More research / larger phase 3 trials with these agents are needed.

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